International Medical Device Conferences
A list of international medical device conferences, medical device meetings and medical device training courses for the medical device industry and in vitro diagnostic medical device industry.
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| DATE | TITLE | LOCATION | ORGANISER |
| March 2010 | |||
| 1-3 | Medical Devices Summit 2010 | Boston, MA, USA |
Opal Events +1 212 532 9898 |
| 1-3 | Principles of European Medical Technology Regulatory Affairs | The Clayton Hotel, Galway, Ireland |
TOPRA +44(0) 20 7510 2560 |
| 2 | Advanced Process Auditing Techniques for Medical Device/Pharma Quality Systems | On-line Event | Compliance Online +1 650 620 3915 |
| 3 | EU's MDD Mod 5 Changes due March 2010 - Impact on CE-mark Compliance | On-line Event | Compliance Online +1 650 620 3915 |
| 3-5 | Advances and Debates in Clinical Obstetrics and Gynaecology | Hurghada, Egypt | Egyptian Society of
Gynaecology and Obstetrics +2 011 700 9620 |
| 18 | How to implement parametric release in EO sterilisation - Practical approach | On-line Event | Compliance Online +1 650 620 3915 |
| 18-19 | Innovative Market Access Strategies for Medical Devices & Technologies | Budapest, Hungary |
NextLevel Pharma +421 232 662 621 |
| 19 | Validating Radiation Sterilisation for medical device industries | On-line Event | Compliance Online +1 650 620 3915 |
| 23-24 | Sterilisation for Medical Devices | London, UK | Informa Lifesciences +44 (0)20 7017 7481 |
| 24 | Overview of the Medical Device Risk Management Standard - ISO 14971 | On-line Event | Compliance Online +1 650 620 3915 |
| 24 | Clinical Evaluation Reports (CERs) Required for All Classes of Medical Devices in Europe | On-line Event | Compliance Online +1 650 620 3915 |
| 26 | Regulatory Requirements for Medical Device Calibration Programs | On-line Event | Compliance Online +1 650 620 3915 |
| 31 | ISO 13485: 2003 for Medical Devices - How it differs to ISO 9001: 2008 and FDA part 820 requirements | On-line Event | Compliance Online +1 650 620 3915 |
| DATE | TITLE | LOCATION | ORGANISER |
| April 2010 | |||
| 9 | ISO 14971: 2007 and the CE Mark | On-line Event | Compliance Online +1 650 620 3915 |
| 12-14 | 7th Annual World Health Care Congress (WHCC) | National Harbor, MD, USA |
World Congress +1 781 939 2587 |
| 13-14 | Clinical Evaluations and Investigations | London, UK | Informa Life Sciences +44 (0)20 7017 7481 |
| 14 | Reducing Ethylene Oxide (EO) Sterilisation costs while maintaining regulatory compliance | On-line Event | Compliance Online +1 650 620 3915 |
| 21-22 | MEDTEC France 2010 | Besançon, France | Canon Communications +33 (0)1 7748 1007 |
| 22 | What are DHF, DMR and DHR? - The FDA Quality Systems Regulations Records Explained | On-line Event | Compliance Online +1 650 620 3915 |
| 29 | The FDA's New Emphasis on Supplier Controls - Is Your Company Ready? | On-line Event | Compliance Online +1 650 620 3915 |
| DATE | TITLE | LOCATION | ORGANISER |
| May 2010 | |||
| 11-13 | Management of Regulatory Affairs and its Contribution to the Medical Technology Lifecycle | Cranfield University, UK |
Cranfield University +44 (0)1234 754192 |
| 20-21 | Device Research - Regulations and Guidelines for Device Clinical Research | San Francisco, CA, USA | Society of Clinical Research Associates +1 800SoCRA92 |
| DATE | TITLE | LOCATION | ORGANISER |
| June 2010 | |||
| 22-24 | Medical Device & IVD Regulations in Asia-Pacific | London, UK | Informa Life Sciences +44 (0)20 7017 7481 |
| DATE | TITLE | LOCATION | ORGANISER |
| September 2010 | |||
| 16-18 | The Pan African Health Expo and Conference 2010 | South Africa | Fair Consultants SA +27 21 713 3360 |
| DATE | TITLE | LOCATION | ORGANISER |
| October 2010 | |||
| 8 | 2010 RAPS Annual Conference & Exhibition | San Jose, CA, USA | Regulatory Affairs Professionals Society (RAPS) +1 301 770 2920 |
| 18-20 | AdvaMed 2010: The MedTech Conference | Washington, DC, USA | AdvaMed +1 202 434 7213 |